Sample information curated by ChIP-Atlas

Antigen

Antigen Class
Input control
Antigen
Input control

Cell type

Cell type Class
Adipocyte
Cell type
Brown preadipocytes
NA
NA

Attributes by original data submitter

Sample

source_name
Brown preadipocyte cell_input DNA
strain background
C57BL/6J
genotype/variation
Mll3-/-;Mll4flox/flox
cell type
imortalized Mll3-/-;Mll4flox/flox brown preadipocytes
stage of adipogenesis
Proliferating (D-3)
infected with
GFP to generate Mll4 KO cells

Sequenced DNA Library

library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Lysates were clarified from sonicated nuclei and protein-DNA complexes were isolated with antibody. Libraries were prepared according to Illumina's instructions accompanying the TruSeq DNA sample prep kit (Cat no. FC-121-2001). Briefly, DNA was end-repaired using a combination of T4 DNA polymerase, Klenow polymerase and T4 polynucleotide kinase. The blunt, phosphorylated ends were treated with Klenow fragment (32 to 52 exo minus) and dATP to yield a protruding 3- 'A' base for ligation of Illumina's adapters which have a single 'T' base overhang at the 3' end. After adapter ligation DNA was PCR amplified with Illumina primers for 15-18 cycles and library fragments of 200-400 bp (insert plus adaptor and PCR primer sequences) were band isolated from an agarose gel. The purified DNA was captured on an Illumina flow cell for cluster generation. Libraries were sequenced on the Genome Analyzer following the manufacturer's protocols.

Sequencing Platform

instrument_model
Illumina HiSeq 2500

mm10

Number of total reads
38818042
Reads aligned (%)
80.3
Duplicates removed (%)
11.6
Number of peaks
447 (qval < 1E-05)

mm9

Number of total reads
38818042
Reads aligned (%)
80.2
Duplicates removed (%)
11.6
Number of peaks
492 (qval < 1E-05)

Base call quality data from DBCLS SRA